160 related articles for article (PubMed ID: 18024694)
1. A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Giaccone G; Di Fede G; Mangieri M; Limido L; Capobianco R; Suardi S; Grisoli M; Binelli S; Fociani P; Bugiani O; Tagliavini F
J Neurol Neurosurg Psychiatry; 2007 Dec; 78(12):1379-82. PubMed ID: 18024694
[TBL] [Abstract][Full Text] [Related]
2. A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Giaccone G; Di Fede G; Mangieri M; Limido L; Capobianco R; Suardi S; Grisoli M; Binelli S; Fociani P; Bugiani O; Tagliavini F
BMJ Case Rep; 2009; 2009():. PubMed ID: 21686549
[TBL] [Abstract][Full Text] [Related]
3. Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease.
Schulz-Schaeffer WJ; Giese A; Windl O; Kretzschmar HA
Clin Neuropathol; 1996; 15(6):353-7. PubMed ID: 8937783
[TBL] [Abstract][Full Text] [Related]
4. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.
Kobayashi A; Parchi P; Yamada M; Mohri S; Kitamoto T
Neuropathology; 2016 Jun; 36(3):305-10. PubMed ID: 26669818
[TBL] [Abstract][Full Text] [Related]
5. A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.
Rodríguez-Martínez AB; Garrido JM; Zarranz JJ; Arteagoitia JM; de Pancorbo MM; Atarés B; Bilbao MJ; Ferrer I; Juste RA
BMC Neurol; 2010 Oct; 10():99. PubMed ID: 20973975
[TBL] [Abstract][Full Text] [Related]
6. Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain.
Puoti G; Giaccone G; Rossi G; Canciani B; Bugiani O; Tagliavini F
Neurology; 1999 Dec; 53(9):2173-6. PubMed ID: 10599800
[TBL] [Abstract][Full Text] [Related]
7. Clinicopathological phenotype of codon 129 valine homozygote sporadic Creutzfeldt-Jakob disease.
Kovacs GG; Head MW; Bunn T; Laszlo L; Will RG; Ironside JW
Neuropathol Appl Neurobiol; 2000 Oct; 26(5):463-72. PubMed ID: 11054187
[TBL] [Abstract][Full Text] [Related]
8. Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.
Pastore M; Chin SS; Bell KL; Dong Z; Yang Q; Yang L; Yuan J; Chen SG; Gambetti P; Zou WQ
Am J Pathol; 2005 Dec; 167(6):1729-38. PubMed ID: 16314483
[TBL] [Abstract][Full Text] [Related]
9. Molecular classification of sporadic Creutzfeldt-Jakob disease.
Hill AF; Joiner S; Wadsworth JD; Sidle KC; Bell JE; Budka H; Ironside JW; Collinge J
Brain; 2003 Jun; 126(Pt 6):1333-46. PubMed ID: 12764055
[TBL] [Abstract][Full Text] [Related]
10. Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
Marcon G; Indaco A; Di Fede G; Suardi S; Finato N; Moretti V; Micoli S; Fociani P; Zerbi P; Pincherle A; Redaelli V; Tagliavini F; Giaccone G
Brain Pathol; 2014 Mar; 24(2):148-51. PubMed ID: 24118545
[TBL] [Abstract][Full Text] [Related]
11. Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone.
Cali I; Miller CJ; Parisi JE; Geschwind MD; Gambetti P; Schonberger LB
Acta Neuropathol Commun; 2015 Jun; 3():37. PubMed ID: 26108478
[TBL] [Abstract][Full Text] [Related]
12. Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature.
Rossi M; Saverioni D; Di Bari M; Baiardi S; Lemstra AW; Pirisinu L; Capellari S; Rozemuller A; Nonno R; Parchi P
Acta Neuropathol Commun; 2017 Nov; 5(1):87. PubMed ID: 29169405
[TBL] [Abstract][Full Text] [Related]
13. Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate.
Kim C; Haldiman T; Cohen Y; Chen W; Blevins J; Sy MS; Cohen M; Safar JG
PLoS Pathog; 2011 Sep; 7(9):e1002242. PubMed ID: 21931554
[TBL] [Abstract][Full Text] [Related]
14. The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients.
Moore RA; Head MW; Ironside JW; Ritchie DL; Zanusso G; Choi YP; Priola SA
PLoS Pathog; 2016 Feb; 12(2):e1005416. PubMed ID: 26840342
[TBL] [Abstract][Full Text] [Related]
15. Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures.
Cassard H; Huor A; Espinosa JC; Douet JY; Lugan S; Aron N; Vilette D; Delisle MB; Marín-Moreno A; Peran P; Beringue V; Torres JM; Ironside JW; Andreoletti O
mBio; 2020 Jun; 11(3):. PubMed ID: 32546613
[TBL] [Abstract][Full Text] [Related]
16. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.
Mitrová E; Belay G
Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632
[TBL] [Abstract][Full Text] [Related]
17. Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British woman.
Mead S; Joiner S; Desbruslais M; Beck JA; O'Donoghue M; Lantos P; Wadsworth JD; Collinge J
Arch Neurol; 2007 Dec; 64(12):1780-4. PubMed ID: 18071044
[TBL] [Abstract][Full Text] [Related]
18. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.
Parchi P; Castellani R; Capellari S; Ghetti B; Young K; Chen SG; Farlow M; Dickson DW; Sima AA; Trojanowski JQ; Petersen RB; Gambetti P
Ann Neurol; 1996 Jun; 39(6):767-78. PubMed ID: 8651649
[TBL] [Abstract][Full Text] [Related]
19. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I
Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565
[TBL] [Abstract][Full Text] [Related]
20. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics.
Cali I; Castellani R; Alshekhlee A; Cohen Y; Blevins J; Yuan J; Langeveld JP; Parchi P; Safar JG; Zou WQ; Gambetti P
Brain; 2009 Oct; 132(Pt 10):2643-58. PubMed ID: 19734292
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
